Peptides

D-a-tert-Butyl-Gly-OH is a leucine derivative.

(S)-2,6-Bis((tert-butoxycarbonyl)amino)hexanoic acid is a polypeptide derivative, can be used to synthesis multifunctional amphiphilic peptide dendrimer, as a nonviral gene vectors, realizes the method in cancer research. (S)-2,6-Bis((tert-butoxycarbonyl)amino)hexanoic acid also involves in the synthesis of an organic substance that increases the luminescence intensity of alkaline phosphatase substrates.

Fmoc-Ser(tBu)-OH is a serine derivative.

Fmoc-Asp(OAll)-OH is an aspartic acid derivative.

Fmoc-D-Ser(tBu)-OH is a serine derivative.

Fmoc-D-Nle-OH is a leucine derivative.

Fmoc-Phe(4-CN)-OH is a phenylalanine derivative.

Fmoc-L-Norleucine is a leucine derivative.

Fmoc-D-Pro-OH is a proline derivative.

Fmoc-His(Trt)-OH has trityl (Trt) group to protect the side-chain of His. Fmoc-His(Trt)-OH has Fmoc group to protect -αNH2. Fmoc-His(Trt)-OH can be used for solid phase synthesis of peptides, providing protection against racemization and by-product formation.

Fmoc-D-Gln(Trt)-OH is a glutamine derivative.

N2-[(9H-Fluoren-9-ylmethoxy)carbonyl]-N-(triphenylmethyl)-D-asparagine is an asparagine derivative.

Fmoc-Asp-OtBu is an aspartic acid derivative.

Fmoc-Cys(Acm)-OH is a cysteine derivative.

Boc-D-3-Pal-OH is an alanine derivative.

H-Gly-Pro-OH is an end product of collagen metabolism that is further cleaved by prolidase.

H-Phg-OH is a Glycine derivative.

Fmoc-Ser(HPO3Bzl)-OH is a serine derivative.

4-Aminobutylphosphonic acid is aamino acids and their derivatives.

N2,N6-Bis(tert-butoxycarbonyl)-D-lysine is a lysine derivative.

Boc-Tyr-OtBu is a tyrosine derivative.

Fmoc-Cpg-OH is a Glycine derivative.

N6-Propionyl-L-lysine is a lysine derivative.

N2-(((9H-Fluoren-9-yl)methoxy)carbonyl)-N6-((4-methoxyphenyl)diphenylmethyl)-L-lysine is a lysine derivative.

6-Chloro-L-tryptophan is a Tryptophan derivative. 6-Chloro-L-tryptophan can be used as a substrate for KtzQ.

L-Phenylalanyl-L-leucine is a leucine derivative.

N-Isobutyrylglycine is a Glycine derivative.

cis-Fmoc-Pro(4-N3)-OH is a proline derivative. cis-Fmoc-Pro(4-N3)-OH is a click chemistry reagent, it contains an Azide group and can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc) with molecules containing Alkyne groups. Strain-promoted alkyne-azide cycloaddition (SPAAC) can also occur with molecules containing DBCO or BCN groups.

VSV-G Peptide is a 11 amino acid peptide derived from the Vesicular Stomatitis viral glycoprotein.

Boc-Asp(OtBu)-OH is an aspartic acid derivative.

(S)-2-((tert-Butoxycarbonyl)amino)-2-cyclohexylacetic acid is a Glycine derivative.

(S)-2-((tert-Butoxycarbonyl)amino)-2-cyclohexylacetic acid is a Glycine derivative.

H-Phe(4-I)-OH is a phenylalanine derivative.

Fmoc-Ser-OH is a serine derivative.

Fmoc-Cys(Trt)-OH is a cysteine derivative.

Fmoc-β-Ala-OH is an alanine derivative.

(S)-2-((tert-Butoxycarbonyl)amino)-3-cyclohexylpropanoic acid is an alanine derivative.

H-Ser(Bzl)-OH is a serine derivative.

H-1-Nal-OH is an alanine derivative.

H-2-Nal-OH is an alanine derivative.

Fmoc-Tle-OH is a leucine derivative.

Fmoc-D-Val-OH is a valine derivative.

Boc-Tyr(Me)-OH is a tyrosine derivative.

Fmoc-Lys(Z)-OH is a lysine derivative.

Fmoc-3-Ala(3-benzothienyl)-OH is an alanine derivative.

SKF 100398 (d(CH2)5Tyr(Et)VAVP), an arginine vasopressin (AVP) analogue, is a specific antagonist of the antidiuretic effect of exogenous and endogenous AVP.

TRV055, a G-protein-biased agonist, is a Gq-biased ligand of the angiotensin II receptor type 1 (AT1R). TRV055 is efficacious in stimulating cellular Gq-mediated signaling.

Ecnoglutide (XW003) is a glucagon-like peptide 1 (GLP-1) receptor agonist.

GRGESP is a collagen gel contraction inhibitor. GRGESP inhibits the spreading of human fibroblasts inside collagen gels and markedly decreased gel contraction. GRGDSP can be used for the research of connective tissue morphogenesis.

Suc-Ala-Glu-Pro-Phe-pNA (Suc-AEPF-pNA) is a chromogenic substrate for the peptidylprolyl isomerase Pin1. Suc-Ala-Glu-Pro-Phe-pNA can be used to evaluate the inhibitory effect of the target compound on Pin1, and catalytic activity of Pin1, etc.